A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579484



Internal ID20952555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114039971..117481220hg38UCSC Ensembl
chr11:113910693..117351935hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg383441250
hg193441243
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229149
Samples
Known GenesAPOA1, APOA4, APOA5, APOC3, BACE1, BACE1-AS, BUD13, C11orf71, CADM1, CEP164, DSCAML1, LINC00900, LOC100652768, NNMT, NXPE1, NXPE2, NXPE4, PAFAH1B2, PCSK7, RBM7, REXO2, RNF214, SIDT2, SIK3, TAGLN, ZBTB16, ZNF259
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579484
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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